• Coordinating day-to-day clinical trial and research study activities. • Implementing study protocol procedures. • Participant recruitment and scheduling.• Scheduling and coordination of study procedures.• Obtaining test results, ensuring that clinicians review them, and completing appropriate documentation.• Developing and implementing patient recruitment plans in conjunction with the marketing team• Maintaining regulatory information for all active… Show more • Coordinating day-to-day clinical trial and research study activities. • Implementing study protocol procedures. • Participant recruitment and scheduling.• Scheduling and coordination of study procedures.• Obtaining test results, ensuring that clinicians review them, and completing appropriate documentation.• Developing and implementing patient recruitment plans in conjunction with the marketing team• Maintaining regulatory information for all active studies.• Preparing IRB required materials as well as compliance and regulatory documents for state and federal agencies and any other pertinent entity.• Responsible for research data management in accordance with protocols established investigators or sponsors. This includes data analysis; data entry; data transfer; data archiving; communication with research collaborators regarding data related study progress, issues, and problems. • Communicating directly with study sponsors, study vendors, and other patient service providers regarding progress of the study and resolving any problems or issues that arise.• Engaging in the pre-screening and screening of potential participants.• Organizing and conducting study start-up and Site initiation visits; as well as study close out.• Screen Donor Egg applicants. Show less

• Developing strategic patient recruiting plans to support the goals and objectives of the CTU. • Responsible for efforts in meeting recruitment and retention goals for clinical research studies, tracking. recruitment status, and developing participant retention strategies.• Presenting to departments within KKI, Johns Hopkins, and Johns Hopkins Bayview; as well as outside healthcare facilities with the goal of introducing the CTU and finding resources for potential… Show more • Developing strategic patient recruiting plans to support the goals and objectives of the CTU. • Responsible for efforts in meeting recruitment and retention goals for clinical research studies, tracking. recruitment status, and developing participant retention strategies.• Presenting to departments within KKI, Johns Hopkins, and Johns Hopkins Bayview; as well as outside healthcare facilities with the goal of introducing the CTU and finding resources for potential participants.• Creating and fostering relationships with clinicians, therapists, social workers, etc. • Coordinating patient recruitment advertising and related events. This includes hosting community forums, tours of the facility, participating in and/or hosting events to disseminate information pertinent to recruitment of participants.• Acting as Lead Coordinator for the CTU’s intake and database project. • Engaging in the pre-screening and screening of potential participants. Show less

• Preparing IRB required materials as well as compliance and regulatory documents for state and federal agencies and any other pertinent entity.• Organizing and conducting study start-up and Site initiation visits; as well as study close out.• Coordinating day to day clinical trial and research study activities. Such as implementing study protocol procedures; participant recruitment and scheduling; scheduling and coordinating of study procedures; obtaining test results, ensuring they… Show more • Preparing IRB required materials as well as compliance and regulatory documents for state and federal agencies and any other pertinent entity.• Organizing and conducting study start-up and Site initiation visits; as well as study close out.• Coordinating day to day clinical trial and research study activities. Such as implementing study protocol procedures; participant recruitment and scheduling; scheduling and coordinating of study procedures; obtaining test results, ensuring they are reviewed by clinicians, and completing appropriate documentation.• Responsible for research data management in accordance with protocols established investigators or sponsors. This includes data analysis; data entry; data transfer; data archiving; communication with research collaborators regarding data related study progress, issues, and problems. • Communicating directly with study sponsors, study vendors, and other patient service providers regarding progress of the study and resolving any problems or issues that arise.• Communicating directly with research collaborators and outside organizations regarding the shipment and receipt of samples, banked samples, and/or data, and resolving any problems or issues that arise.• Preparing, compiling, documenting, and presenting results of ongoing studies for conference and meeting presentations, peer reviewed manuscripts, and poster submissions and grants. Show less

Full service financial services firm providing insurance, securities and investments for business owners, individuals and groups.

I specialized in selling personal lines of insurance (home, auto and life insurance) to individuals in Delaware and Maryland.